Difference between revisions of "Part:BBa K1139150"
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To characterize the function of the <i>RM/lac</i> hybrid promoter (<partinfo>BBa_K1139151</partinfo>), we constructed this part PRM/lac-GFP (<partinfo>BBa_K1139150</partinfo>) by inserting ''RM/lac'' promoter upstream of a GFP coding sequence. By using reporter cells that contain PRM/lac-GFP, we measured the fluorescence intensity of the cells induced by CI and IPTG (Fig. 2). <br>  
 
To characterize the function of the <i>RM/lac</i> hybrid promoter (<partinfo>BBa_K1139151</partinfo>), we constructed this part PRM/lac-GFP (<partinfo>BBa_K1139150</partinfo>) by inserting ''RM/lac'' promoter upstream of a GFP coding sequence. By using reporter cells that contain PRM/lac-GFP, we measured the fluorescence intensity of the cells induced by CI and IPTG (Fig. 2). <br>  
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We saw that our new ''RM/lac'' hybrid promoter was actually activated by CI and repressed by LacI through an induction assay (Fig. 3).<br>
+
We confirmed that our new ''RM/lac'' hybrid promoter was actually activated by CI through an induction assay (Fig. 3).<br>
  
 
[[Image:titech2013_parts_K1139150_main_Fig2.jpg|thumb|left|310px|<b>Fig. 2.</b> Fluorescence intensity detected by flow cytometer]]
 
[[Image:titech2013_parts_K1139150_main_Fig2.jpg|thumb|left|310px|<b>Fig. 2.</b> Fluorescence intensity detected by flow cytometer]]

Revision as of 21:47, 28 October 2013

Prm/lac-GFP-TT

PRM/lac is a hybrid promoter that is activated by lamda repressor (CI) and repressed by LacI repressor (Fig. 1).
On the downstream of the promoter, GFP is inserted as a reporter.

Fig. 1. Our newly designed hybrid promoter

To characterize the function of the RM/lac hybrid promoter (BBa_K1139151), we constructed this part PRM/lac-GFP (BBa_K1139150) by inserting RM/lac promoter upstream of a GFP coding sequence. By using reporter cells that contain PRM/lac-GFP, we measured the fluorescence intensity of the cells induced by CI and IPTG (Fig. 2).
We confirmed that our new RM/lac hybrid promoter was actually activated by CI through an induction assay (Fig. 3).

Fig. 2. Fluorescence intensity detected by flow cytometer
Fig. 3. Comparison of N99 and JM2.300


For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/RM-lac_Hybrid_Promoter_Assay our work in Tokyo_Tech 2013 wiki].

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 769